rs1276352833, FGA

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Dysfibrinogenemia
CUI: C1260903
Disease: Dysfibrinogenemia
6 0.925 0.080 4 154586057 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2016 2016
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.925 0.080 4 154586057 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2016 2016